<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Journal Article</dc:product_type><dc:title>Learning-accelerated discovery of immune-tumour interactions</dc:title><dc:creator>Ozik, Jonathan; Collier, Nicholson; Heiland, Randy; An, Gary; Macklin, Paul</dc:creator><dc:corporate_author/><dc:editor/><dc:description>We present an integrated framework for enabling dynamic exploration of design spaces for cancer immunotherapies with detailed dynamical simulation models on high-performance computing resources. Our framework combines PhysiCell, an open source agent-based simulation platform for cancer and other multicellular systems, and EMEWS, an open source platform for extreme-scale model exploration. We build an agent-based model of immunosurveillance against heterogeneous tumours, which includes spatial dynamics of stochastic tumour–immune contact interactions. We implement active learning and genetic algorithms using high-performance computing workflows to adaptively sample the model parameter space and iteratively discover optimal cancer regression regions within biological and clinical constraints.</dc:description><dc:publisher/><dc:date>2019-08-05</dc:date><dc:nsf_par_id>10188156</dc:nsf_par_id><dc:journal_name>Molecular Systems Design &amp; Engineering</dc:journal_name><dc:journal_volume>4</dc:journal_volume><dc:journal_issue>4</dc:journal_issue><dc:page_range_or_elocation>747 to 760</dc:page_range_or_elocation><dc:issn>2058-9689</dc:issn><dc:isbn/><dc:doi>https://doi.org/10.1039/c9me00036d</dc:doi><dcq:identifierAwardId>1720625</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>